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rs118192185

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118192185(A;G)
Make rs118192185(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position63472463
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs118192185
ebirs118192185
HLIrs118192185
Exacrs118192185
Varsomers118192185
Maprs118192185
PheGenIrs118192185
hapmaprs118192185
1000 genomesrs118192185
hgdprs118192185
ensemblrs118192185
gopubmedrs118192185
geneviewrs118192185
scholarrs118192185
googlers118192185
pharmgkbrs118192185
gwascentralrs118192185
openSNPrs118192185
23andMers118192185
23andMe allrs118192185
SNP Nexus

SNPshotrs118192185
SNPdbers118192185
MSV3drs118192185
GWAS Ctlgrs118192185
Max Magnitude0
ClinVar
Risk rs118192185(G;G)
Alt rs118192185(G;G)
Reference rs118192185(A;A)
Significance Pathogenic
Disease Benign familial neonatal seizures 1
Variation info
Gene KCNQ2
CLNDBN Benign familial neonatal seizures 1
Reversed 1
HGVS NC_000020.10:g.62103816T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000020982.1,


OMIM121200
Desc
Variant
Relatedalso